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Figure 10 in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Figure 10. – Annual thermal cycle for different life phases of Z. asper. The "gametogenesis" phase starts when temperatures fall in September and continues throughout the winter but slows down in November when the temperature reaches 5°C. This period of time at 5°C, indicated as "vernalization" on the graph, lasts from November to February. The duration of this period is very important because it directly conditions the success of the reproduction. Rapid and regular rising of temperatures to 10°C triggers reproduction from the beginning of March and continues until the end of April.
Figure 3. – A in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Figure 3. – A: Growth curve of the Z. asper group born in captivity (2008) descended from wild Z. asper from the Beaume. At 2 years old, some fish could not be sexed but all Z. asper were mature at 3 years and monitoring of both sexes was possible. At 5 years old, females are significantly longer than males. B: Quantity of food per week for 20 asper (Beaume 2008) in 2015. When the temperature reaches 14 to 15°C in May, Z. asper consume 3 times the quantity of food eaten at 5 to 10°C. From 20°C in July, consumption levels are more than 5 times higher than in the winter.
Figure 9. – A in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Figure 9. – A: Comparison of incubation results as a function of cold period length from 30 to 120 days. More than 64,000 eggs were collected during these trials and all egg clutches were accurately counted at four key moments of the incubation process: on laying, at 10 days, at transfer for hatching and at hatching. From the first development stages, egg mortality declines as the length of the winter cold period increases. B: Clutch by clutch detail of the incubation survival rate of eggs for batches of "Beaume" broodstock subjected to 3 different temperature periods. The egg clutches produced during the same experiment are identified by an identical colour. Within the same group, survival rate results sometimes varied widely. The hatching rates for broodstock subjected to 90 days of vernalization are the most variable. This wide variability suggests that the 90-day period of cold temperatures creates a boundary, which determines whether reproduction is successful or not. C: Variation in hatching rate (mean and standard deviation) as a function of vernalization period length. Unlike those from the "Beaume" stock, Z. asper of "Durance" stock we used in 2016 and 2017 (captured in 2015 and 2016), were replaced between the two years. The hatching rate varies in accordance with the duration of the cold period experienced by the broodstock during the winter. For the "Beaume" broodstock, Kruskal-Wallis tests show that comparisons between the results obtained with the 120-day period and the other periods are significant (p <0.05). The length of the vernalization period clearly has an influence on the hatching rate. This test was also applied to data from the experiments involving both sets of stock and 120-day periods. As this test was not significant (p = 0.07), it demonstrates that both sets of stock reacted similarly to this vernalization period.
Figure 2 in SYNOPSIS OF BEGONIA (BEGONIACEAE) FROM THE NORTHERN ARM OF SULAWESI AND SANGIHE ISLAND, INDONESIA, INCLUDING THREE NEW SPECIES
Figure 2. Distribution maps of Begonia species occurring on the northern arm of Sulawesi. Distribution points are from georeferenced collections from major herbarium collections (B, BO, E, K, KRB, L, SING), the Begonia Resource Centre (Hughes et al., 2015–) and the Sulawesi Begonia Data Portal (Thomas et al., 2013, continuously updated).
Figure 12. Begonia rieckei. A in SYNOPSIS OF BEGONIA (BEGONIACEAE) FROM THE NORTHERN ARM OF SULAWESI AND SANGIHE ISLAND, INDONESIA, INCLUDING THREE NEW SPECIES
Figure 12. Begonia rieckei. A, Habit, reddish leaves with white dots along the margin and between the veins; B, inflorescence; C, male flowers; D, female flower; E and F, infructescence; G, ovary (crosssection of middle part). A from W.H. Ardi WI410; B, D and F from W.H. Ardi WI207; C, E and G from W.H. Ardi WI391. Photographs: W. H. Ardi.
Supporting Dataset (Tables S1-S7, Figure S1) for "Heavy-mineral grain counting: Counting techniques, error estimation, and the number of grains to be counted"
<p>This Dataset comprises Tables S1-S7 for the article <strong>"Heavy-mineral grain counting: Counting techniques, error estimation, and the number of grains to be counted"</strong> authored by Jan Schönig and submitted to J<em>ournal of Geophysical Research: Earth Surface</em>.</p> <p>Figure S1: Error of different counting methods in comparison with theory and without considering the finite population correction</p> <p>Table S1: Heavy-mineral dataset from semi-automated Raman analysis</p> <p>Table S2: Summary of heavy-mineral composition for individual samples in percent</p> <p>Table S3: Computed ribbon compositions for individual samples and ribbon sizes given in numbers of counts</p> <p>Table S4: Relative errors at 95 % quantile for consecutive ribbon counting simulations</p> <p>Table S5: Relative errors at 95 % quantile for maximum distance ribbon counting simulations</p> <p>Table S6: Relative errors at 95 % quantile for cluster counting simulations</p> <p>Table S7: Numerical solution for determining the number of counts required to discriminate the content of two mineral species in an aliquot</p>
An unusual pulse shape change event in PSR J1713+0747 observed with the Green Bank Telescope and CHIME: Profile data and figure reproduction scripts
<p>This Zenodo entry contains data used in the paper "An unusual pulse shape change event in PSR J1713+0747 observed with the Green Bank Telescope and CHIME", to be published in The Astrophysical Journal. This includes minimally processed profile data in PSRFITS format, as well as pulsar ephemerides (.par files), time-of-arrival estimates (.tim files), and scripts which can be used to reproduce the figures and tables in the paper. For more information, see README.md.</p>
Figure 2 in Characterization of Eugenia uniflora accessions: a native species with great commercial potential in America
Figure 2. Collection sites of the 40 Surinam Cherry accessions in the state of Rio Grande do Sul with the cluster according to genetic similarity obtained with RAPD markers. Group I =; Group II =; Group III =).
Figure 1 in Characterization of Eugenia uniflora accessions: a native species with great commercial potential in America
Figure 1. Dendrogram of genetic similarity between the 40 Surinam Cherry, obtained from RAPD markers. The line indicates the 84% cut-off point based on the average similarity between populations.
Figure 3 in Trichocline maxima (Compositae, Mutisieae) a rare Pampean daisy rediscovered after 70 years in Uruguay
Figure 3. Distribution map of Trichocline maxima. The orange dot represents the latest record of the species that is reported in this work. The black dot in Uruguay is from collections cited in the additional examined material section. The black dot in Brazil represents the possible location of Malme's (1931) citation of a Sellow's collection: Inter Rio Pardo et Bagé.
Figure 1. A-G. Trichocline maxima. A in Trichocline maxima (Compositae, Mutisieae) a rare Pampean daisy rediscovered after 70 years in Uruguay
Figure 1. A-G. Trichocline maxima. A. General view of the species habit; B. Capitulum; C. Involucre; D. Detail of achene and pappus; E. Detail of rosette leaves, scapes and xylopodium; F. Detail of the rosette and lobate leaves; G. Habitat. Photos credits: A-C, F and G by José M. Bonifacino; D by Fábio P. Torchelsen.
Figures 18–26, Barynema species. 18–20, B in Review of the Australian endemic odontocerid genus Barynema and status of Australian Marilia (Trichoptera)
Figures 18–26, Barynema species. 18–20, B. lobatum sp. nov.: 18, holotype male, Queensland, Montville, 27.ix.1955, (NMV Tri-27064), genitalia ventral; 19, paratype male (NMV 27120), lateral; 20, paratype female (NMV TRI-27063) terminalia, ventral. 21–24, B. dilatum sp. nov.: 21–23, holotype, male (NMV WTH-2966, PT-2033) genitalia ventral, lateral, and dorsal, respectively; 24, paratype female (Python Creek NMV), terminalia, ventral. 25, 26, B. dolabratum sp. nov. holotype male, (Oliver Creek NMV), genitalia, ventral and lateral, respectively. Abbreviations: api. lob. = apical lobe; d. lob. = dorsal lobe of inferior appendages; har. = harpago; ph. = phallus; pre. app. = pre-anal appendages; up. p. = upper penis cover.
Figure 12. Amutatiola macroventosa n. gen. & n in Two new genera and species of sepioline squids (Cephalopoda: Sepiolidae) from Australia
Figure 12. Amutatiola macroventosa n. gen. & n. sp.: a, spermatophore, holotype (MOV F80081) Spermatophore length, 3.55 mm (insets: i, close-up of oral cap; ii, close-up of cement body); b, Bursa copulatrix, paratype 1 (MOV F275293; black scale: 1 mm/division) (lflc: left funnel locking cartilage; lg: left gill); arrow points to the bursa copulatrix entrance.
Figure 17 in Microscopic analysis of the developing dentition in the pouch young of the extinct marsupial Thylacinus cynocephalus, with an assessment of other developmental stages and eruption
Figure 17. Selected dentaries of Thylacinus showing differences in the diastemata between the premolars as the effect of increasing age. A, subadult (in labial view) with m3 erupted, but not m4. Only slight suggestions of diastemata are evident between the premolars; B (lingual view) and C (labial view), showing later stages of m4 eruption and the increase of diastemata in adults.
Figure 2. Dextrasepiola taenia n. gen. & n in Two new genera and species of sepioline squids (Cephalopoda: Sepiolidae) from Australia
Figure 2. Dextrasepiola taenia n. gen. & n. sp., female, paratype 1 (MOV F91359): a, dorsal view; b, ventral view; c, oral view of arm crown showing sucker arrangements of female.
Figure 16 in Microscopic analysis of the developing dentition in the pouch young of the extinct marsupial Thylacinus cynocephalus, with an assessment of other developmental stages and eruption
Figure 16. Later stages of early eruption in Thylacinus showing the presence and early loss of dp3 in the dentary. A, Part of the dentary (CU A6 7/10), redrawn from Moeller (1968), showing the erupted dp3, the unerupted successor p3 in its alveolar crypt, immediately anterior to dp3, and the erupting m1. The erupting dp1 and dp2 are also labeled; B, A slightly later stage of eruption in the dentary (USNM 115365) shows that the dp3 has been lost, and successor p3 is in early eruption. The m1 is now almost completely erupted. c indicates lower successional canine in B.
Figure 5. Dextrasepiola taenia n. gen. & n in Two new genera and species of sepioline squids (Cephalopoda: Sepiolidae) from Australia
Figure 5. Dextrasepiola taenia n. gen. & n. sp. (grids in background: 1 mm × 1 mm): a, spermatophore from the holotype (MOV F80458); b, close-up of cement body; c, bursa copulatrix, paratype 1 (MOV F31359; bc: bursa copulatrix; rg: right gill; rsf: right side of funnel); d, bursa copulatrix, juvenile (MOV F31360; bc: bursa copulatrix; lflc: left funnel locking cartilage; rflc: right funnel locking cartilage; rg: right gill); e, bursa copulatrix, paratype 3 (MOV F31361; bc: bursa copulatrix; lsf: left side of funnel; ms: mantle septum; rsf: right side of funnel); f, close-up of a portion of e, arrow points to opening of bursa copulatrix.
Figure 13 in Microscopic analysis of the developing dentition in the pouch young of the extinct marsupial Thylacinus cynocephalus, with an assessment of other developmental stages and eruption
Figure 13. Computed tomography images from the supplementary data of Newton et al. (2018). A, section of the skull and dentition from TMAG A931, a thylacine pouch young of 35 - 37 days old; B, Section of the skull and dentition from TMAG A930, a thylacine pouch young of 66 - 67 days old. Scale bars are 5 mm. C, canine; dP1, deciduous first premolar; dP2, deciduous second premolar; dP3, deciduous third premolar; M1, first molar; P3, successional third premolar.
Figure 9. Amutatiola macroventosa n. gen. & n in Two new genera and species of sepioline squids (Cephalopoda: Sepiolidae) from Australia
Figure 9. Amutatiola macroventosa n. gen. & n. sp. male, paratype 5 (MOV F158244). Oral views of arms (grids in background: 1 mm × 1 mm): a, right arm I; b, right arm II; c, right arm III; d, right arm IV; e, left arm I; f, left arm II; g, left arm III; h, left arm IV.
Figure 12 in Microscopic analysis of the developing dentition in the pouch young of the extinct marsupial Thylacinus cynocephalus, with an assessment of other developmental stages and eruption
Figure 12. Section through dp3 and its successor p3. Only a small fragment of the lingual successional lamina is evident. Compare this single section with the camera lucida drawings in Figure 11. dp3, deciduous third premolar; lsl, lingual successional lamina; p3, successional third premolar.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.